Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos

Detalhes bibliográficos
Autor(a) principal: Peres, Kenya C. [UNESP]
Data de Publicação: 2015
Outros Autores: Trinca, Vitor [UNESP], Oliveira, Fernanda P. [UNESP], Oliveira, Lilian J., Bressan, Fabiana F., Pimentel, Jose R. V., Meirelles, Flavio V., Pereira, Flávia Thomaz Verechia [UNESP]
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2015000500477&lng=en&nrm=iso&tlng=en
http://hdl.handle.net/11449/129676
Resumo: The transgenic application of green fluorescent protein (GFP) as fetal cell marker on cattle cloned placenta could provide an exclusive model for studying the morphologic and immunologic maternal-fetal interactions, providing information about its mapping, distinguishing the fetal from maternal cells. This model will have direct application, mainly because these animals present problems during its development. With this model's support, we intend to verify the substances transport between mother and fetus during endocytosis, through the immunolocalization of protein named caveolae. For these, we used 06 cloned bovine and 30 cattle samples of artificial insemination (AI) with 90 days of pregnancy, which had been their development interrupted by humanitarian slaughter of the recipient and recovery of the pregnant uterus. We collected the placentome and the chorion. A part of the samples was cut and fixed, by immersion, on a solution containing 4% of parafomaldehyde or 10% of formaldehyde on a sodium phosphate buffer (PBS), at 0,1 M pH 7.4, Zamboni solution (4% of paraformaldehyde, 15% of picric acid, on sodium phosphate buffer 0,1 M pH 7.4), metacarn (60% of metanol, 30% of chloroform, and 10% glacial acetic acid), for morphologic and immunohistochemistry verification for caveolinas proteins -1 and -2 (CAV -1 and CAV-2). The caveolins -1 were found in fetal and maternal villi, but its strongest staining was observed in the endometrial stroma. The caveolins -2 had positive staining in trophoblast and chorioallantoic membrane, and specifically in giant trophoblastic binucleated cell. Therefore the results were compared between cloned cattle and from AI or natural mating, for assisting on detection of the reason of many placental alterations, embryonic losses, spontaneous abortion, post-natal mortality and large offspring syndrome on laboratory-manipulated animals. The result suggests that the proteins caveolins -1 and -2 (CAV-1 and CAV-2) are part of the caveolae composition and important structures related to the molecule transfer to the fetus, nourish it through endocytosis and pinocytosis.
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spelling Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicosCaracterization of caveolin -1 and -2 proteins in cloned and transgenic placenta of cattleCaveolin-1 and-2 proteinsCaveolaePlacentationImmunolocalizationCattleProteínas caveolinas -1 e -2Placenta de conceptos bovinos clonadosTransgênicosCavéolaCaveolinaPlacentaçãoImunolocalizaçãoThe transgenic application of green fluorescent protein (GFP) as fetal cell marker on cattle cloned placenta could provide an exclusive model for studying the morphologic and immunologic maternal-fetal interactions, providing information about its mapping, distinguishing the fetal from maternal cells. This model will have direct application, mainly because these animals present problems during its development. With this model's support, we intend to verify the substances transport between mother and fetus during endocytosis, through the immunolocalization of protein named caveolae. For these, we used 06 cloned bovine and 30 cattle samples of artificial insemination (AI) with 90 days of pregnancy, which had been their development interrupted by humanitarian slaughter of the recipient and recovery of the pregnant uterus. We collected the placentome and the chorion. A part of the samples was cut and fixed, by immersion, on a solution containing 4% of parafomaldehyde or 10% of formaldehyde on a sodium phosphate buffer (PBS), at 0,1 M pH 7.4, Zamboni solution (4% of paraformaldehyde, 15% of picric acid, on sodium phosphate buffer 0,1 M pH 7.4), metacarn (60% of metanol, 30% of chloroform, and 10% glacial acetic acid), for morphologic and immunohistochemistry verification for caveolinas proteins -1 and -2 (CAV -1 and CAV-2). The caveolins -1 were found in fetal and maternal villi, but its strongest staining was observed in the endometrial stroma. The caveolins -2 had positive staining in trophoblast and chorioallantoic membrane, and specifically in giant trophoblastic binucleated cell. Therefore the results were compared between cloned cattle and from AI or natural mating, for assisting on detection of the reason of many placental alterations, embryonic losses, spontaneous abortion, post-natal mortality and large offspring syndrome on laboratory-manipulated animals. The result suggests that the proteins caveolins -1 and -2 (CAV-1 and CAV-2) are part of the caveolae composition and important structures related to the molecule transfer to the fetus, nourish it through endocytosis and pinocytosis.A utilização da transgenia com a proteína fluorescente verde (GFP) como marcador de células de origem fetal nas placentas de clones bovinos servirá de modelo inédito para estudo morfofisiológico e imunológico da interação materno-fetal, visto que possibilitará o seu mapeamento, diferenciando as células fetais das maternas. Tal modelo terá aplicação direta, principalmente porque estes são animais que apresentam problemas em relação ao seu desenvolvimento. Com o auxílio deste modelo, pretende-se verificar o transporte de substâncias entre a mãe e o feto via endocitose, pela imunolocalização das proteínas chamadas de caveolinas. Para tanto foram utilizados 06 bovinos clonados e 30 bovinos de inseminação artificial (IA) com idade até 90 dias de gestação, os quais tiveram seu desenvolvimento interrompido mediante abate humanitário das receptoras e ovariosalpingohisterectomia, com posterior recuperação do útero gestante. Foram coletados os placentônios e o cório. Uma parte das amostras foi recortada e fixada, por imersão, em solução de parafolmaldeído a 4% ou formoldeído a 10% em tampão fosfato de sódio (PBS) a 0,1M pH 7.4, solução de Zamboni (4% de paraformoldeído, 15% de ácido pícrico, em tampão fosfato de sódio a 0,1M pH 7.4), metacarn (60% de metanol, 30% de clorofórmio, e 10% de ácido acético glacial), para verificação da morfologia e realização de imuno-histoquímica para as proteínas caveolinas -1 e -2 (CAV -1 e CAV-2). As caveolinas -1 foram localizadas nos vilos fetais e maternos, mas sua marcação mais forte foi observada no estroma endometrial. As caveolinas -2 tiveram marcação positiva no trofoblasto e membrana córioalantoide, e, especificamente em célula trofoblástica gigante binucleada. Sendo assim, os resultados mostram que a proteína CAV-1 teve uma maior expressão em relação à proteína CAV-2 e que as proteínas CAV-1 e -2 são parte da composição das cavéolas, sendo estruturas importantes e relacionadas com a transferência de moléculas para o feto, realizando a nutrição do mesmo mediante endocitose e pinocitose.Univ Estadual Paulista Julio de Mesquita Filho Un, Lab Morfofisiol Placenta &Embriao, BR-17900000 Dracena, SP, BrazilMichigan State Univ, Dept Anim Sci, E Lansing, MI 48824 USAUniv Sao Paulo, Fac Zootecnia &Engn Alimentos, Lab Morfofisiol Mol Desenvolvimento, BR-13635900 Pirassununga, SP, BrazilUniv Estadual Paulista Julio de Mesquita Filho, Lab Morfofisiol Placenta & Embriao, BR-17900000 Dracena, SP, BrazilRevista Pesquisa Veterinaria BrasileiraUniversidade Estadual Paulista (Unesp)Michigan State UnivUniversidade de São Paulo (USP)Peres, Kenya C. [UNESP]Trinca, Vitor [UNESP]Oliveira, Fernanda P. [UNESP]Oliveira, Lilian J.Bressan, Fabiana F.Pimentel, Jose R. V.Meirelles, Flavio V.Pereira, Flávia Thomaz Verechia [UNESP]2015-10-22T06:28:22Z2015-10-22T06:28:22Z2015-05-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article477-485application/pdfhttp://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2015000500477&lng=en&nrm=iso&tlng=enPesquisa Veterinaria Brasileira, v. 35, n. 5, p. 477-485, 2015.0100-736Xhttp://hdl.handle.net/11449/12967610.1590/S0100-736X-2015000500016S0100-736X2015000500477WOS:000357746000016S0100-736X2015000500477.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPporPesquisa Veterinaria Brasileira0.385info:eu-repo/semantics/openAccess2024-05-07T13:59:32Zoai:repositorio.unesp.br:11449/129676Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T13:58:46.030144Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos
Caracterization of caveolin -1 and -2 proteins in cloned and transgenic placenta of cattle
title Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos
spellingShingle Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos
Peres, Kenya C. [UNESP]
Caveolin-1 and-2 proteins
Caveolae
Placentation
Immunolocalization
Cattle
Proteínas caveolinas -1 e -2
Placenta de conceptos bovinos clonados
Transgênicos
Cavéola
Caveolina
Placentação
Imunolocalização
title_short Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos
title_full Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos
title_fullStr Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos
title_full_unstemmed Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos
title_sort Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos
author Peres, Kenya C. [UNESP]
author_facet Peres, Kenya C. [UNESP]
Trinca, Vitor [UNESP]
Oliveira, Fernanda P. [UNESP]
Oliveira, Lilian J.
Bressan, Fabiana F.
Pimentel, Jose R. V.
Meirelles, Flavio V.
Pereira, Flávia Thomaz Verechia [UNESP]
author_role author
author2 Trinca, Vitor [UNESP]
Oliveira, Fernanda P. [UNESP]
Oliveira, Lilian J.
Bressan, Fabiana F.
Pimentel, Jose R. V.
Meirelles, Flavio V.
Pereira, Flávia Thomaz Verechia [UNESP]
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Michigan State Univ
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Peres, Kenya C. [UNESP]
Trinca, Vitor [UNESP]
Oliveira, Fernanda P. [UNESP]
Oliveira, Lilian J.
Bressan, Fabiana F.
Pimentel, Jose R. V.
Meirelles, Flavio V.
Pereira, Flávia Thomaz Verechia [UNESP]
dc.subject.por.fl_str_mv Caveolin-1 and-2 proteins
Caveolae
Placentation
Immunolocalization
Cattle
Proteínas caveolinas -1 e -2
Placenta de conceptos bovinos clonados
Transgênicos
Cavéola
Caveolina
Placentação
Imunolocalização
topic Caveolin-1 and-2 proteins
Caveolae
Placentation
Immunolocalization
Cattle
Proteínas caveolinas -1 e -2
Placenta de conceptos bovinos clonados
Transgênicos
Cavéola
Caveolina
Placentação
Imunolocalização
description The transgenic application of green fluorescent protein (GFP) as fetal cell marker on cattle cloned placenta could provide an exclusive model for studying the morphologic and immunologic maternal-fetal interactions, providing information about its mapping, distinguishing the fetal from maternal cells. This model will have direct application, mainly because these animals present problems during its development. With this model's support, we intend to verify the substances transport between mother and fetus during endocytosis, through the immunolocalization of protein named caveolae. For these, we used 06 cloned bovine and 30 cattle samples of artificial insemination (AI) with 90 days of pregnancy, which had been their development interrupted by humanitarian slaughter of the recipient and recovery of the pregnant uterus. We collected the placentome and the chorion. A part of the samples was cut and fixed, by immersion, on a solution containing 4% of parafomaldehyde or 10% of formaldehyde on a sodium phosphate buffer (PBS), at 0,1 M pH 7.4, Zamboni solution (4% of paraformaldehyde, 15% of picric acid, on sodium phosphate buffer 0,1 M pH 7.4), metacarn (60% of metanol, 30% of chloroform, and 10% glacial acetic acid), for morphologic and immunohistochemistry verification for caveolinas proteins -1 and -2 (CAV -1 and CAV-2). The caveolins -1 were found in fetal and maternal villi, but its strongest staining was observed in the endometrial stroma. The caveolins -2 had positive staining in trophoblast and chorioallantoic membrane, and specifically in giant trophoblastic binucleated cell. Therefore the results were compared between cloned cattle and from AI or natural mating, for assisting on detection of the reason of many placental alterations, embryonic losses, spontaneous abortion, post-natal mortality and large offspring syndrome on laboratory-manipulated animals. The result suggests that the proteins caveolins -1 and -2 (CAV-1 and CAV-2) are part of the caveolae composition and important structures related to the molecule transfer to the fetus, nourish it through endocytosis and pinocytosis.
publishDate 2015
dc.date.none.fl_str_mv 2015-10-22T06:28:22Z
2015-10-22T06:28:22Z
2015-05-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2015000500477&lng=en&nrm=iso&tlng=en
Pesquisa Veterinaria Brasileira, v. 35, n. 5, p. 477-485, 2015.
0100-736X
http://hdl.handle.net/11449/129676
10.1590/S0100-736X-2015000500016
S0100-736X2015000500477
WOS:000357746000016
S0100-736X2015000500477.pdf
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2015000500477&lng=en&nrm=iso&tlng=en
http://hdl.handle.net/11449/129676
identifier_str_mv Pesquisa Veterinaria Brasileira, v. 35, n. 5, p. 477-485, 2015.
0100-736X
10.1590/S0100-736X-2015000500016
S0100-736X2015000500477
WOS:000357746000016
S0100-736X2015000500477.pdf
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Pesquisa Veterinaria Brasileira
0.385
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv 477-485
application/pdf
dc.publisher.none.fl_str_mv Revista Pesquisa Veterinaria Brasileira
publisher.none.fl_str_mv Revista Pesquisa Veterinaria Brasileira
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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